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American Journal of Medical Genetics|October 2, 1996
Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1M K Wirtz, J R Samples, P L Kramer, et al.American Journal of Medical Genetics|January 20, 1997
Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patientF Y Choy, M L Humphries, P FerreiraAmerican Journal of Medical Genetics|January 20, 1997
De novo trisomy 16pJ L Carrasco Juan, J C Cigudosa, A Otero Gómez, et al.American Journal of Medical Genetics|January 20, 1997
Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13A Tar, A Ion, J Sólyom, et al.American Journal of Medical Genetics|February 21, 1997
Comparison of the family history with the family study method: report from the Camberwell Collaborative Psychosis StudyN J Davies, P C Sham, C Gilvarry, et al.American Journal of Medical Genetics|February 21, 1997
Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndromeC L Barr, K G Wigg, E Zovko, et al.American Journal of Medical Genetics|February 21, 1997
Bias in the genomic distribution of CAG and CTG trinucleotide repeatsM C O'Donovan, C GuyAmerican Journal of Medical Genetics|February 11, 1997
Are blastogenetic anomalies sporadic?M L Martínez-Frías, J L FríasAmerican Journal of Medical Genetics|February 11, 1997
Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?O Reish, R J Gorlin, M Hordinsky, et al.American Journal of Medical Genetics|February 11, 1997
Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl geneS M Kleyman, A J Parekh, A R Rodriguez, et al.Pageof 854